Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26130 | A01 | 14516047 | G | A | missense_variant | MODERATE | c.800C>T|p.Thr267Ile |
S126 |
2 | BAA01g26130 | A01 | 14516315 | G | A | missense_variant | MODERATE | c.532C>T|p.Leu178Phe |
S63 |
3 | BAA01g26130 | A01 | 14516443 | G | A | missense_variant | MODERATE | c.404C>T|p.Ala135Val |
S37 |
4 | BAA01g26130 | A01 | 14516532 | A | T | missense_variant | MODERATE | c.315T>A|p.Asn105Lys |
S13 |
5 | BAA01g26130 | A01 | 14516631 | G | A | synonymous_variant | LOW | c.216C>T|p.Phe72Phe |
S186 |
6 | BAA01g26130 | A01 | 14516896 | G | A | upstream_gene_variant | MODIFIER | c.-50C>T| |
S191 |
7 | BAA01g26130 | A01 | 14517186 | C | T | upstream_gene_variant | MODIFIER | c.-340G>A| |
S242 |
8 | BAA01g26130 | A01 | 14518814 | C | T | upstream_gene_variant | MODIFIER | c.-1968G>A| |
S51 |
9 | BAA01g26130 | A01 | 14519027 | G | A | upstream_gene_variant | MODIFIER | c.-2181C>T| |
S56 |
10 | BAA01g26130 | A01 | 14519363 | G | A | upstream_gene_variant | MODIFIER | c.-2517C>T| |
S175 |
11 | BAA01g26130 | A01 | 14520147 | C | T | upstream_gene_variant | MODIFIER | c.-3301G>A| |
S112 |
12 | BAA01g26130 | A01 | 14520227 | G | A | upstream_gene_variant | MODIFIER | c.-3381C>T| |
S293 |
13 | BAA01g26130 | A01 | 14521094 | C | T | upstream_gene_variant | MODIFIER | c.-4248G>A| |
S146 |
14 | BAA01g26130 | A01 | 14521210 | G | A | upstream_gene_variant | MODIFIER | c.-4364C>T| |
S144 |
15 | BAA01g26130 | A01 | 14521710 | G | A | upstream_gene_variant | MODIFIER | c.-4864C>T| |
S287 |
16 | BAA01g26130 | A01 | 14521811 | G | A | upstream_gene_variant | MODIFIER | c.-4965C>T| |
S86 |